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MAO-B-IN-7
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
MAO-B-IN-7图片
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
MAO-B-IN-7 是一种有效且具有血脑屏障渗透性的MAO-BAChE抑制剂,对人 AChE、电鳗 AChE 和 MAO-B 的IC50分别为 41 nM、87 nM 和 0.3 μM。MAO-B-IN-7 能有效缓解氧化应激和神经炎症损伤。
生物活性

MAO-B-IN-7 is a potent and blood-brain barrier permeableMAO-BandAChEinhibitor withIC50s of 41 nM, 87 nM and 0.3 μM for humanAChE, electric eelAChEandMAO-B, respectively. MAO-B-IN-7 can effectively alleviate oxidative stress and neuroinflammatory damage[1].

IC50& Target[1]

MAO-B

0.3 μM (IC50)

hAChE

41 nM (IC50)

体外研究
(In Vitro)

MAO-B-IN-7 (compound 7d) can effectively interact with Cu2+to form the corresponding complexes, and has good ability to inhibit ROS’s production induced by Cu2+[1].
MAO-B-IN-7 (10-100 μM; 24 hours) decreases the viability of PC-12 cells at 100 μM, but does not show obvious cytotoxicity at 10 and 25 μM[1].
MAO-B-IN-7 (4-25 μM; 24 hours) protects H2O2-induced PC-12 cells injury, and the cell viability are 80.2%, 71.1% and 56.3% at 25.0 μM, 10.0 μM and 4.0 μM, respectively.[1].
MAO-B-IN-7 (2.5 μM and 10 μM; 8 and 24 hours) inhibits ROS production induced by LPS in BV-2 cells in a dose-dependent manner; inhibits NO production with 30.4%, 43.5% and 58.9% at the concentrations of 0.5 μM, 2.5 μM and 10.0 μM, respectively; also inhibits TNF-α release with 32.7%, 47.8% and 63.2% at the concentrations of μM, 2.5 μM and 10.0 μM, respectively[1].
MAO-B-IN-7 exhibits the parallel artificial membrane permeation of 8.59 × 10-6in vitroblood-brain barrier permeation study[1].

Cell Cytotoxicity Assay

Cell Line:PC-12[1]
Concentration:10 μM, 25 μM, 100 μM
Incubation Time:24 hours
Result:Decreased the viability of PC-12 cells at 100 μM.
分子量

409.52

Formula

C25H31NO4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.